Oral infection with Porphyromonas gingivalis induces peri-implantitis in a murine model: Evaluation of bone loss and the local inflammatory response

被引:56
作者
Tzach-Nahman, Rinat [1 ,2 ]
Mizraji, Gabriel [1 ,2 ]
Shapira, Lior [1 ]
Nussbaum, Gabriel [2 ]
Wilensky, Asaf [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Ctr, Fac Dent Med, Dept Periodontol, Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Ctr, Fac Dent Med, Inst Dent Sci, Jerusalem, Israel
关键词
cytokines; murine; peri-implantitis; periodontitis; residual bone volume; PERIODONTITIS; PROGRESSION; ACTIVATION; MICROBIOTA; MUCOSITIS; BIOFILM; LESIONS; TEETH; TLR2;
D O I
10.1111/jcpe.12735
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
AimPeri-implantitis is a major health concern, with unclear pathogenesis, and with no accessible animal models. Our aim was to establish a mouse model for peri-implantitis and to investigate mediators of inflammation. Materials and MethodsMice were divided into implanted versus non-implanted groups. Implants were inserted immediately following the extraction of the upper first molar. Four weeks following implantation, implanted and non-implanted mice were challenged with either Porphyromonas gingivalis or vehicle (eight mice in each subgroup, 32 mice in total). Alveolar bone loss and expression of inflammatory mediators in the soft tissue were assessed 42days following infection. ResultsPorphyromonas gingivalis infection induced greater bone loss around implants than around teeth. In non-infected animals, the presence of the implant correlated with elevated expression of Il-10, Foxp3 and Rankl/Opg ratio, while Tnf- levels were decreased relative to tissue around teeth. Six weeks following infection, Tnf- increased significantly while the expression of Foxp3 decreased in the tissue around the implants. No significant differences in anti- or pro-inflammatory mediators were found around teeth of infected, relative to non-infected mice. ConclusionsOral infection with P.gingivalis of mice with implants induced bone loss and a shift in gingival cytokine expression. This mouse model enables exploration of the pathogenesis of peri-implantitis and testing of novel treatments.
引用
收藏
页码:739 / 748
页数:10
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